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OTC Naproxen and Acetaminophen Anti-Inflammatory Action in Dental Implant Patients

Demonstration of OTC Naproxen Sodium's (Aleve's) Anti-inflammatory Action in Dental Implant Surgery Patients

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04694300
Enrollment
30
Registered
2021-01-05
Start date
2021-02-07
Completion date
2022-08-28
Last updated
2024-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osseointegrated Dental Implantation, Pain, Acute

Keywords

Naproxen sodium, Acetaminophen, Postsurgical dental pain, Prostaglandins, Interleukins

Brief summary

This double-blind pilot study will evaluate the anti-inflammatory and analgesic effects of an over-the-counter (OTC) regimen of naproxen sodium versus acetaminophen in patients receiving one or two (adjacent) dental implants. It will also confirm that naproxen sodium in the OTC dosage range is a good alternative to immediate-release opioid formulations, which are subject to misuse, abuse and diversion in this patient population.

Detailed description

Placement of dental implants is a frequently performed outpatient surgical procedure, with United States dentists currently placing implants in approximately 500,000 patients per year.This procedure has become the gold standard for replacing missing teeth due to its high level of predictability and patient acceptance, with long-term success rates greater than 95%. Thus, the number of patients opting for this procedure over dentures and fixed bridges continues to increase. In the period between 1999 and 2000 only 0.7% of the USA population had missing teeth with implants in contrast to 5.7% between 2015 and 2016 It is estimated that by 2026, if the current pace of dental implant placement continues, approximately 17% of the population will have dental implants. Dental implant surgery involves the incision of gingival tissue to expose the underlying bone, followed by the creation of a precise bony cavity where the implant will be placed using a specialized surgical drill, and lastly the screwing of the implant into bone using a specialized handpiece Thus, it is not surprising that post-surgical pain is a common sequela following dental implant surgery. Patients often experience post-surgical pain for several days after the placement of one to three dental implants, but at a pain intensity level that is generally less than that of dental impaction surgery. This post-surgical pain is inflammatory in nature; thus, NSAIDs have demonstrated efficacy and are the preferred analgesics in this patient population. Postoperative administration of intranasal ketorolac (SPRIX®) and oral acetaminophen 325 mg plus codeine 30 mg have both demonstrated efficacy. The soft tissue and bony trauma associated with dental implant surgery upregulates inflammatory mediators both locally and systemically. Elevated levels of interleukin (IL)-6, IL-8, and macrophage inflammatory protein (MIP)-1β have been observed in gingival crevicular fluid (GCF) from the implant site and the adjacent teeth one week after surgery. Prostaglandin E2 has been measured in the GCF of teeth surrounding implant sites employing similar methodology. Additionally, standard periodontal flap and bony recontouring surgery, which shares many similarities to dental implant surgery, induces an upregulation in immunoreactive prostaglandin E2 and leukotriene B4 levels at the surgical site. Dental implant surgery also increases cytokine levels in plasma, indicative of a systemic inflammatory response. Thus, in addition to being a model to study the efficacy and tolerability of OTC analgesics, dental implant surgery also appears to be an excellent model to study the anti-inflammatory properties of NSAIDs such as naproxen sodium. Therefore, the investigators propose to initiate a double-blind, pilot study to evaluate the anti-inflammatory and analgesic effects of an OTC regimen of naproxen sodium versus acetaminophen in dental implant surgery patients. Notably, the vast majority of these patients are over the age of 45, a patient demographic that is rarely captured in postsurgical dental pain studies. Compared to dental impaction surgery patients, implant surgery patients possess more comorbidities such as hypertension, hyperlipidemia and hyperglycemia Thus, while dental impaction patients are typically on few if any drugs, polypharmacy is more of the norm in dental implant surgery patients. Performing a controlled study with OTC naproxen sodium in this population will provide the opportunity to confirm that its short-term use is generally safe and effective in these older, more medically complex patients. It will also confirm that naproxen sodium in the OTC dosage range is a good alternative to immediate-release opioid formulations, which are subject to misuse, abuse and diversion in this patient population.

Interventions

DRUGNaproxen

440 mg by mouth immediately after completion of implant surgery followed by 220 mg 12 hours later. Then 220 mg every 8 hours for the next two days.

DRUGAcetaminophen

1000 mg by mouth immediately after the completion of implant surgery followed by 1000 mg every 6 hours for 3 days after surgery with a maximum daily dose of 3000 mg.

DRUGTramadol

50 mg by mouth every 6 hours as needed for pain

Sponsors

University of Pennsylvania
CollaboratorOTHER
Hersh, Elliot V., DMD, MS, PhD
Lead SponsorINDIV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Administration of naproxen or acetaminophen will be masked by over-encapsulation

Intervention model description

Double blind, randomized, active-controlled, two arms

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Subject requires surgical placement of one or two (adjacent) dental implants * Ability to read and sign informed consent * Males and females for 18-75 years of age * Non-smokers * Negative urine drug screen

Exclusion criteria

* Advanced periodontal disease (\>20% Clinical Attachment Loss \>20% radiographic bone loss) * History of bisphosphonate usage * Medical history or medical condition that makes any of the study medications (naproxen sodium, acetaminophen, tramadol, etc.) inappropriate treatment options including any scheduled or recent cardiac procedures (within 6 months), a history of GI ulcers, liver or kidney disease, and anticoagulant or lithium intake. * History of an allergic reaction to any pain reliever/fever reducer * Contraindication to opioid use * Positive urine drug screen for drugs of abuse unless on stable doses of a non-analgesic drug for a legitimate medical purpose * Pregnancy - A urine pregnancy test will be performed immediately before the scheduled surgery on all women of child-bearing potential * Local or systemic diseases that affects wound healing and inflammatory biomarkers (diabetes, autoimmune (rheumatoid arthritis), or inflammatory disorders - osteoarthritis is allowed). * Smokers on this pilot study because it can affect levels of inflammatory biomarkers - a urine cotinine test will be performed immediately prior to the scheduled surgery on all subjects even if participant denies smoking history * History of systemic steroid use over 2 weeks within last 2 years. * Poor oral hygiene on a non-compliant individual.

Design outcomes

Primary

MeasureTime frameDescription
Pain Intensity Scores on Numeric Pain Intensity Scale 0-6 HoursUp to 6 hoursMedian maximum pain intensity scores where 0 = no pain and 10 = worst possible pain
Pain Intensity Scores From 6 Through 72 Hours (Multi-dose Phase)6-72 hours Post initial DosePain intensity scores where 0 = no pain and 10 = worst possible pain
Peak Plasma IL-6 Concentrations6 hoursPlasma IL-6 concentrations 6 hours after treatment measured by ELISA
Plasma IL-6 Change From Baseline6 hours post dosePercent change in plasma IL-6 levels at 6 hours after treatment relative to baseline

Secondary

MeasureTime frameDescription
COX-2 Activity6 hours post-doseCOX-2 activity was evaluated ex vivo by quantifying plasma prostaglandin (PG)E2 levels following lipopolysaccharide (LPS) stimulation in whole blood,
Rescue Analgesic Use0-6 hoursNumber of patients requiring opioid rescue medication (tramadol) during inpatient phase (0-6 hours) in each treatment group
Peak GCF IL-8levels24 hours post-doseLevels of IL-8 in gingival crevicular fluid measured at 24 hours after treatment
Rescue Medication Use Outpatient Phase (6-72 Hours)6-72 hoursNumber of patients requiring opioid rescue medication during outpatient phase in both treatment groups
Peak GCF IL-1β Levels24 hours post-doseLevels of IL-1β in gingival crevicular fluid measured at 24 hours after treatment
COX-1 Activity Percent of Baseline (Pre-surgery)6 hours post doseCyclooxygenase (COX)-1 activity was evaluated ex vivo by quantifying serum thromboxane B2 levels

Countries

United States

Participant flow

Recruitment details

Subjects scheduled in University of Pennsylvania School of Dental Medicine Periodontics Clinic to receive the surgical placement of one or two dental implants.

Participants by arm

ArmCount
Naproxen Sodium
Naproxen: 440 mg by mouth immediately after completion of implant surgery followed by 220 mg 12 hours later. Then 220 mg every 8 hours for the next two days. Tramadol: 50 mg by mouth every 6 hours as needed for pain
15
Acetaminophen
Acetaminophen: 1000 mg by mouth immediately after the completion of implant surgery followed by 1000 mg every 6 hours for 3 days after surgery with a maximum daily dose of 3000 mg. Tramadol: 50 mg by mouth every 6 hours as needed for pain
15
Total30

Baseline characteristics

CharacteristicTotalAcetaminophenNaproxen Sodium
Age, Continuous46.2 years
STANDARD_DEVIATION 14.3
45.5 years
STANDARD_DEVIATION 14.2
46.8 years
STANDARD_DEVIATION 14.9
Body Mass Index (BMI)26.0 BMI (kg/m^2)
STANDARD_DEVIATION 4
26.8 BMI (kg/m^2)
STANDARD_DEVIATION 4.3
25.2 BMI (kg/m^2)
STANDARD_DEVIATION 3.6
Ethnicity (NIH/OMB)
Hispanic or Latino
2 Participants1 Participants1 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
28 Participants14 Participants14 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Length of Surgery78.4 Minutes
STANDARD_DEVIATION 33.7
85.5 Minutes
STANDARD_DEVIATION 30.6
71.1 Minutes
STANDARD_DEVIATION 35.8
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
4 Participants2 Participants2 Participants
Race (NIH/OMB)
Black or African American
14 Participants10 Participants4 Participants
Race (NIH/OMB)
More than one race
1 Participants0 Participants1 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
11 Participants3 Participants8 Participants
Sex: Female, Male
Female
18 Participants11 Participants7 Participants
Sex: Female, Male
Male
12 Participants4 Participants8 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 150 / 15
other
Total, other adverse events
1 / 152 / 15
serious
Total, serious adverse events
0 / 150 / 15

Outcome results

Primary

Pain Intensity Scores From 6 Through 72 Hours (Multi-dose Phase)

Pain intensity scores where 0 = no pain and 10 = worst possible pain

Time frame: 6-72 hours Post initial Dose

Population: Mean Pain Intensity Scores from 6-72 hours Following Around-the-Clock Dosing With Naproxen Sodium or Acetaminophen

ArmMeasureValue (MEAN)
Naproxen SodiumPain Intensity Scores From 6 Through 72 Hours (Multi-dose Phase)0.3 units on pain intensity scale
AcetaminophenPain Intensity Scores From 6 Through 72 Hours (Multi-dose Phase)1.7 units on pain intensity scale
p-value: <0.05Wilcoxon (Mann-Whitney)
Primary

Pain Intensity Scores on Numeric Pain Intensity Scale 0-6 Hours

Median maximum pain intensity scores where 0 = no pain and 10 = worst possible pain

Time frame: Up to 6 hours

Population: Medium Greatest Pain Intensity Scores from 0-6 hours Following Dosing With Naproxen Sodium or Acetaminophen

ArmMeasureValue (MEDIAN)
Naproxen SodiumPain Intensity Scores on Numeric Pain Intensity Scale 0-6 Hours1 score on a scale
AcetaminophenPain Intensity Scores on Numeric Pain Intensity Scale 0-6 Hours3 score on a scale
p-value: <0.05Wilcoxon (Mann-Whitney)
Primary

Peak Plasma IL-6 Concentrations

Plasma IL-6 concentrations 6 hours after treatment measured by ELISA

Time frame: 6 hours

ArmMeasureValue (MEDIAN)
Naproxen SodiumPeak Plasma IL-6 Concentrations6.5 pg/ml
AcetaminophenPeak Plasma IL-6 Concentrations12.1 pg/ml
p-value: 0.12Wilcoxon (Mann-Whitney)
Primary

Plasma IL-6 Change From Baseline

Percent change in plasma IL-6 levels at 6 hours after treatment relative to baseline

Time frame: 6 hours post dose

ArmMeasureValue (MEDIAN)
Naproxen SodiumPlasma IL-6 Change From Baseline276.9 percentage change from baseline
AcetaminophenPlasma IL-6 Change From Baseline519.1 percentage change from baseline
p-value: <0.05Wilcoxon (Mann-Whitney)
Secondary

COX-1 Activity Percent of Baseline (Pre-surgery)

Cyclooxygenase (COX)-1 activity was evaluated ex vivo by quantifying serum thromboxane B2 levels

Time frame: 6 hours post dose

ArmMeasureValue (MEDIAN)
Naproxen SodiumCOX-1 Activity Percent of Baseline (Pre-surgery)3.7 percentage of baseline blood levels
AcetaminophenCOX-1 Activity Percent of Baseline (Pre-surgery)77.4 percentage of baseline blood levels
p-value: <0.05Wilcoxon (Mann-Whitney)
Secondary

COX-2 Activity

COX-2 activity was evaluated ex vivo by quantifying plasma prostaglandin (PG)E2 levels following lipopolysaccharide (LPS) stimulation in whole blood,

Time frame: 6 hours post-dose

Population: Patient in each group surgically receiving one or two implants

ArmMeasureValue (MEDIAN)
Naproxen SodiumCOX-2 Activity48.4 percentage of baseline blood levels
AcetaminophenCOX-2 Activity52.4 percentage of baseline blood levels
p-value: 0.59Wilcoxon (Mann-Whitney)
Secondary

Peak GCF IL-1β Levels

Levels of IL-1β in gingival crevicular fluid measured at 24 hours after treatment

Time frame: 24 hours post-dose

ArmMeasureValue (MEDIAN)
Naproxen SodiumPeak GCF IL-1β Levels263 pg/ml
AcetaminophenPeak GCF IL-1β Levels456 pg/ml
p-value: 0.29Wilcoxon (Mann-Whitney)
Secondary

Peak GCF IL-8levels

Levels of IL-8 in gingival crevicular fluid measured at 24 hours after treatment

Time frame: 24 hours post-dose

ArmMeasureValue (MEDIAN)
Naproxen SodiumPeak GCF IL-8levels2962 pg/ml
AcetaminophenPeak GCF IL-8levels5729 pg/ml
p-value: 0.14Wilcoxon (Mann-Whitney)
Secondary

Rescue Analgesic Use

Number of patients requiring opioid rescue medication (tramadol) during inpatient phase (0-6 hours) in each treatment group

Time frame: 0-6 hours

Population: Number of patients in each treatment group requiring opioid rescue medication (tramadol) during inpatient phase (0-6 hours)

ArmMeasureValue (NUMBER)
Naproxen SodiumRescue Analgesic Use0 participants
AcetaminophenRescue Analgesic Use3 participants
Secondary

Rescue Medication Use Outpatient Phase (6-72 Hours)

Number of patients requiring opioid rescue medication during outpatient phase in both treatment groups

Time frame: 6-72 hours

ArmMeasureValue (NUMBER)
Naproxen SodiumRescue Medication Use Outpatient Phase (6-72 Hours)2 participants
AcetaminophenRescue Medication Use Outpatient Phase (6-72 Hours)5 participants

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026